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rs878855196

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855196(-;-)
Make rs878855196(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position64807912
GeneMEN1
is asnp
is mentioned by
dbSNPrs878855196
ebirs878855196
HLIrs878855196
Exacrs878855196
Varsomers878855196
Maprs878855196
PheGenIrs878855196
hapmaprs878855196
1000 genomesrs878855196
hgdprs878855196
ensemblrs878855196
gopubmedrs878855196
geneviewrs878855196
scholarrs878855196
googlers878855196
pharmgkbrs878855196
gwascentralrs878855196
openSNPrs878855196
23andMers878855196
23andMe allrs878855196
SNP Nexus

SNPshotrs878855196
SNPdbers878855196
MSV3drs878855196
GWAS Ctlgrs878855196
Max Magnitude0
ClinVar
Risk rs878855196(;)
Alt rs878855196(;)
Reference rs878855196(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64575384delG
CLNSRC
CLNACC RCV000232633.1,